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59 result(s) for "Pellissier, Hélène"
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Chiral Copper Catalysis in Enantioselective Domino Reactions
This review updates the field of enantioselective copper-catalysed domino reactions promoted by chiral green copper catalysts, covering the literature since 2017. These complexes are derived from a diversity of chiral ligands, including mostly bisoxazolines and biphosphines along with monophosphines, N-heterocyclic carbenes, proline derivatives, phosphoric acids, phosphoramidates, and different types of N,N-ligands. The review shows that asymmetric copper catalysis, that suits the growing demand for greener processes, offers a real opportunity to replace toxic and expensive metals in the near future.
Synthesis of chiral 3-substituted 3-amino-2-oxindoles through enantioselective catalytic nucleophilic additions to isatin imines
This review collects the recent developments in the synthesis of chiral 3-substituted 3-amino-2-oxindoles based on enantioselective catalytic nucleophilic additions to isatin imines published since the beginning of 2015.
Recent Developments in the Catalytic Enantioselective Sakurai Reaction
The Sakurai reaction constitutes a valuable tool for carbon–carbon bond formation. The use of nontoxic allylic reagents as well as the atom economy of the global process has prompted the development of enantioselective (aza)-variants based on the use of chiral organo- and metal catalysts. This review collects the recent developments in catalytic enantioselective Sakurai reactions published since the beginning of 2011, including methodologies based on the use of chiral organocatalysts, metal/boron catalysts and multicatalyst systems. It is divided into three parts, dealing successively with enantioselective organocatalytic (aza)-Sakurai reactions, enantioselective metal/boron-catalyzed Sakurai reactions and enantioselective multicatalyzed (aza)-Sakurai reactions. It shows that, although still widely developed with aromatic aldehydes, the enantioselective catalytic Sakurai reaction has considerably matured in the last decade.
Recent developments in the asymmetric Reformatsky-type reaction
This review collects the most important developments in asymmetric Reformatsky-type reactions published since the beginning of 2013, including both diastereoselective methodologies based on the use of chiral substrates and enantioselective catalytic procedures.
Asymmetric Synthesis of Three-Membered Rings
The first handbook to focus on the asymmetric synthesis of different types of three-membered rings. The outstanding and experienced authors have an excellent international reputation and cover cyclopropanes, epoxides and aziridines as well as chiral oxaziridines in equal measure. To this end, they describe in detail different synthetic approaches starting with chiral substrates as well as the application of chiral metal- or organocatalysts. Furthermore, methods for the kinetic resolution of initially racemic products are treated alongside recent advances and novel developments in established techniques for the synthesis of three-membered rings.
Recent Developments in Enantioselective Scandium-Catalyzed Transformations
This review collects the recent developments in the field of enantioselective scandium-catalyzed transformations published since the beginning of 2016, illustrating the power of chiral scandium catalysts to promote all types of reactions.
Enantioselective Cobalt-Catalysed Transformations
With a foreword from leading organic chemist Professor Paul Wender, this book collects the major developments reported in the past thirty years in the field of enantioselective reactions promoted by chiral cobalt catalysts.
Chirality from dynamic kinetic resolution
The last 15 years have witnessed significant developments in the efficiency and scope of the application of DKR. These now offer a serious alternative to conventional methods for asymmetric synthesis. Indeed, impressive examples using new enzymes and major progress in the DKR of racemates have taken place over the past few years. The powerful combination of enzymes and metals has also been the subject of spectacular development. In addition, a new type of DKR, involving organocatalysts, has recently appeared. Although asymmetric catalysis has undergone development during the last two decades, the most common industrial process used to obtain enantiomerically pure compounds is still via resolution of racemic mixtures. This is despite the major disadvantage that only a maximum of 50% product yield can be obtained. It is not surprising that DKR, which solves the problem of the limitation in yield, has attracted an increasing amount of interest from both the industrial and the academic perspective. This book provides an up-date on the principle methods employed to obtain dynamic kinetic resolution (DKR) by either enzymatic or non-enzymatic methods. It also illustrates the diversity of useful chiral products that can be obtained through this powerful concept. Divided into three sections, the book deals successively with non-enzymatic methods, enzymatic methods, and the use of transition metals and enzymes in tandem.
Recent developments in asymmetric organocatalysis
The aim of this book is to cover the very recent developments in asymmetric organocatalysis, focussing on those published since the beginning of 2008. The last decade has witnessed an explosive growth in the field of asymmetric organocatalysis with an impressive amount of new catalysts, novel methodologies, and applications in numerous reaction types, such as nucleophilic substitutions, addition reactions, as well as cycloadditions, oxidations, reductions, kinetic resolutions, and miscellaneous reactions. This very diverse and intensely developing field is too wide to cover in a single review. The timeliness of the book together with the expected impact is excellent, since nowadays asymmetric organocatalysis is arguably the most intensively developed field in organic chemistry. The book is designed to meet the demands of a postgraduate textbook, containing case studies and Q&A sections, as well as a practical book filled with facts and data useful as a working tool for the practitioner. The book is divided into ten sections, dealing successively with nucleophilic additions to electron-deficient C=C double bonds, nucleophilic additions to C=O double bonds, nucleophilic additions to C=N double bonds, nucleophilic additions to unsaturated nitrogen, nucleophilic substitutions at aliphatic carbon, cycloaddition reactions, oxidations, reductions, kinetic resolutions and desymmetrisations, and miscellaneous reactions.